Association of CLEC16A with human common variable immunodeficiency disorder and role in murine B cells

Publikation

Association of CLEC16A with human common variable immunodeficiency disorder and role in murine B cells

Wissenschaftlicher Artikel/Review - 20.04.2015

Li Jin, Gieger Christian, Nöthen Markus M, Büning Carsten, Brand Stephan, Sullivan Kathleen E, Orange Jordan S, Fevang Børre, Schreiber Stefan, Lieb Wolfgang, Aukrust Pål, Chapel Helen, Cunningham-Rundles Charlotte, Franke Andre, Karlsen Tom H, Grimbacher Bodo, Hakonarson Hakon, Hammarström Lennart, Winkelmann Juliane, Nair Rajan P, Elder James T, Jørgensen Silje F, Maggadottir S Melkorka, Bakay Marina, Warnatz Klaus, Glessner Joseph, Pandey Rahul, Salzer Ulrich, Schmidt Reinhold E, Perez Elena, Resnick Elena, Goldacker Sigune, Buchta Mary, Witte Torsten, Padyukov Leonid, Videm Vibeke, Folseraas Trine, Atschekzei Faranaz, Ellinghaus Eva

Zitation

Li J, Gieger C, Nöthen M, Büning C, Brand S, Sullivan K, Orange J, Fevang B, Schreiber S, Lieb W, Aukrust P, Chapel H, Cunningham-Rundles C, Franke A, Karlsen T, Grimbacher B, Hakonarson H, Hammarström L, Winkelmann J, Nair R, Elder J, Jørgensen S, Maggadottir S, Bakay M, Warnatz K, Glessner J, Pandey R, Salzer U, Schmidt R, Perez E, Resnick E, Goldacker S, Buchta M, Witte T, Padyukov L, Videm V, Folseraas T, Atschekzei F, Ellinghaus E. Association of CLEC16A with human common variable immunodeficiency disorder and role in murine B cells. Nat Commun 2015; 6:6804.

Art

Wissenschaftlicher Artikel/Review (Englisch)

Zeitschrift

Nat Commun 2015; 6

Veröffentlichungsdatum

20.04.2015

eISSN (Online)

2041-1723

Seiten

6804

Kurzbeschreibung/Zielsetzung

Common variable immunodeficiency disorder (CVID) is the most common symptomatic primary immunodeficiency in adults, characterized by B-cell abnormalities and inadequate antibody response. CVID patients have considerable autoimmune comorbidity and we therefore hypothesized that genetic susceptibility to CVID may overlap with autoimmune disorders. Here, in the largest genetic study performed in CVID to date, we compare 778 CVID cases with 10,999 controls across 123,127 single-nucleotide polymorphisms (SNPs) on the Immunochip. We identify the first non-HLA genome-wide significant risk locus at CLEC16A (rs17806056, P=2.0 × 10(-9)) and confirm the previously reported human leukocyte antigen (HLA) associations on chromosome 6p21 (rs1049225, P=4.8 × 10(-16)). Clec16a knockdown (KD) mice showed reduced number of B cells and elevated IgM levels compared with controls, suggesting that CLEC16A may be involved in immune regulatory pathways of relevance to CVID. In conclusion, the CLEC16A associations in CVID represent the first robust evidence of non-HLA associations in this immunodeficiency condition.